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[Mechanism of modified Liangge San in treatment of acute respiratory distress syndrome based on network pharmacology and experimental validation].
Li, Quan; Wang, Meng-Meng; Nie, Shi-Nan; Sun, Hai-Jun; Tang, Cheng; Sun, Zhao-Rui.
Afiliación
  • Li Q; Nanjing University of Chinese Medicine Nanjing 210023, China Department of Critical Care Medicine, Suqian First Hospital Suqian 223800, China.
  • Wang MM; Department of Emergency Medicine, Jinling Hospital(General Hospital of Eastern Theater Command), Medical School of Nanjing University Nanjing 210002, China.
  • Nie SN; Nanjing University of Chinese Medicine Nanjing 210023, China Department of Emergency Medicine, Jinling Hospital(General Hospital of Eastern Theater Command), Medical School of Nanjing University Nanjing 210002, China.
  • Sun HJ; Department of Critical Care Medicine, Suqian First Hospital Suqian 223800, China.
  • Tang C; Department of Critical Care Medicine, Suqian First Hospital Suqian 223800, China.
  • Sun ZR; Nanjing University of Chinese Medicine Nanjing 210023, China Department of Emergency Medicine, Jinling Hospital(General Hospital of Eastern Theater Command), Medical School of Nanjing University Nanjing 210002, China.
Zhongguo Zhong Yao Za Zhi ; 47(24): 6753-6762, 2022 Dec.
Article en Zh | MEDLINE | ID: mdl-36604925
A network pharmacology-based strategy combined with molecular docking and in vitro validation was employed to investigate potential targets and molecular mechanisms of modified Liangge San(MLGS) against acute respiratory distress syndrome(ARDS). Active ingredients and corresponding targets of MLGS were screened out on the Traditional Chinese Medicines Systems Pharmacology(TCMSP) database, and the disease targets of ARDS were obtained by integrating GeneCards and DisGeNET database. The two were intersected to obtain the potential targets of MLGS against ARDS. Cytoscape 3.7.2 was used to construct a "Chinese medicine-active ingredient-target network" of MLGS and a "regulatory network of MLGS against ARDS". The protein-protein interaction(PPI) network was created on the STRING database platform, and the Metascape database was used to carry out Gene Ontology(GO) function enrichment analysis and Kyoto Encyclopedia of Genes and Genomes(KEGG) pathway enrichment analysis. Subsequently, molecular docking and in vitro experiments were performed to further verify the above findings. A total of 211 active ingredients of MLGS and 54 key targets were obtained. The GO enrichment analysis obtained 709 GO entries(P<0.05), including 457 biological processes(BP), 50 cell components(CC), and 98 molecular functions(MF), mainly involved in lipopolysaccharides, response to reactive oxygen species, and apoptosis signal pathways. KEGG pathway enrichment analysis obtained 266 pathways, mainly involved in the cancer signaling pathways, advanced glycation end-products and their receptors(AGE-RAGE) signaling pathways, fluid shear stress, atherosclerosis, proteoglycan pathway in cancer, nuclear and factor kappa B(NF-κB) signaling pathway. Molecular docking showed that the main active ingredients bound steadily with the targets. The experiments proved that MLGS inhibited the generation of reactive oxygen species and the activation of NF-κB signaling pathway, thereby reducing apoptosis. The study shows that MLGS, through its multiple active ingredients including wogonin and luteolin, can treat ARDS by intervening in various signaling pathways such as NF-κB, inhibiting the inflammatory response and oxidative stress, and reducing apoptosis.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndrome de Dificultad Respiratoria / Medicamentos Herbarios Chinos Tipo de estudio: Diagnostic_studies Idioma: Zh Revista: Zhongguo Zhong Yao Za Zhi Asunto de la revista: FARMACOLOGIA / TERAPIAS COMPLEMENTARES Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndrome de Dificultad Respiratoria / Medicamentos Herbarios Chinos Tipo de estudio: Diagnostic_studies Idioma: Zh Revista: Zhongguo Zhong Yao Za Zhi Asunto de la revista: FARMACOLOGIA / TERAPIAS COMPLEMENTARES Año: 2022 Tipo del documento: Article